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rs794728924

From SNPedia

Orientationminus
Geno Mag Summary
(TCTG;TCTG) 0 common in clinvar
Make rs794728924(-;-)
Make rs794728924(-;TCTG)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38550905
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728924
ebirs794728924
HLIrs794728924
Exacrs794728924
Varsomers794728924
Maprs794728924
PheGenIrs794728924
hapmaprs794728924
1000 genomesrs794728924
hgdprs794728924
ensemblrs794728924
gopubmedrs794728924
geneviewrs794728924
scholarrs794728924
googlers794728924
pharmgkbrs794728924
gwascentralrs794728924
openSNPrs794728924
23andMers794728924
23andMe allrs794728924
SNP Nexus

SNPshotrs794728924
SNPdbers794728924
MSV3drs794728924
GWAS Ctlgrs794728924
Max Magnitude0
ClinVar
Risk rs794728924(;)
Alt rs794728924(;)
Reference rs794728924(TCTG;TCTG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38592396_38592399delCAGA
CLNSRC
CLNACC RCV000183167.2,